Medical Device Regulatory Affairs Jobs in Lake Forest, IL

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Regulatory Affairs Specialist  

GForce Life Sciences - Lake Forest, IL, United States

combination of education and experience. 4+ years’ experience in Regulatory Affairs role. Strong knowledge of IVDR and EU regulatory requirements is required. 1+ years’ experience in an IVD or medical device

from: linkedin.com - 11 days ago

Marketing Manager  

Abbott Laboratories - Lake Forest, IL

Policy requirements and all EHS requirements. Collaborate with internal and external stakeholders to achieve objectives, including but not limited to the field sales force, legal, regulatory, medical USD 95,000.00 - 190,000.00 per year

from: Dice.com (+1 source) - 6 days ago

Sr. Specialist - Cybersecurity, Regulatory Affairs  

Sysmex - Lincolnshire, Illinois

software and cybersecurity framework and procedures to maintain and ensure compliance with medical device regulatory requirements. The individual will coordinate and collect specific product registration

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from: resume-library.com - 5 days ago

Manager, Regulatory Affairs  

Sysmex - Lincolnshire, Illinois

Affairs contributes to the regulatory strategy for new and modified Sysmex medical device products. The individual will need to identify, assess and communicate regulatory development, submission strategies

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from: resume-library.com - 9 days ago

Senior Manager, Medical Affairs Quality ( On-site, IL based)  

North Chicago, IL

regulatory commitments., covering the AbbVie drug, device and cosmetic portfolio. The role reports to a Director of Safety, Vigilance and Medical Affairs Quality Assurance. There is an expectation

from: Pharmadiversityjobboard.com - 24 days ago

Director US Regulatory Global Strategic Labelling - Remote Opportunity  

Lundbeck - Deerfield, Illinois

). REQUIRED EDUCATION, EXPERIENCE AND SKILLS: Accredited Bachelor's Degree 10+ years of experience within a pharm aceutical, medical device and/o r biotech industry, with 7+ years of experience in Regulatory

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from: resume-library.com (+1 source) - Yesterday

Director, Safety. Regulatory Affairs and Medical Affairs Quality Standards  

AbbVie - North Chicago, Illinois

is responsible for the management of a RDQA global Safety, Regulatory Affairs (RA) and Medical Affairs (MA) QA team which provides independent quality oversight of GxP activities, covering the AbbVie drug, device

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from: resume-library.com - 18 days ago

Senior Counsel, Regulatory  

Baxter International Inc - Deerfield, Illinois, USA

projects, transactions, or matters. Serves relevant business leadership and other law department members as a key advisor in defined areas of medical device and pharmaceutical regulatory law. In addition $216,000 to $324,000

from: Ivyexec.com - 10 days ago

Senior Manager, Medical Affairs Quality ( On-site, IL based)  

AbbVie - North Chicago, Illinois

, including but not limited to non-interventional studies, medical information and other regulatory commitments., covering the AbbVie drug, device and cosmetic portfolio. The role reports to a Director

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from: resume-library.com - 24 days ago

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Associate Director VYEPTI Consumer Marketing  

Lundbeck - Deerfield, IL

through collaboration and communication with: brand leadership, data & analytics, market research, sales training, finance, regulatory affairs, product communications, and other cross-functional partners

from: Pharmadiversityjobboard.com (+1 source) - 9 days ago


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